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Exome sequencing identifies a CHKB mutation in Spanish patient with megaconial congenital muscular dystrophy and mtDNA depletion.

By Arenas Barbero, Joaquín | Martín, Miguel A. | Martinez Azorin, Francisco | Delmiro Magdalena, Aitor. European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society, 2014 . 18(6):796-800. , Formato Vancouver: Castro-Gago M, Dacruz-Alvárez D, Pintos-Martínez E, Beiras-Iglesias A, Delmiro A, Arenas J et al. Exome sequencing identifies a CHKB mutation in Spanish patient with megaconial congenital muscular dystrophy and mtDNA depletion. Eur J Paediatr Neurol. 2014 Nov;18(6):796-800.

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Differential proteomic profiling unveils new molecular mechanisms associated with mitochondrial complex III deficiency.

By Marín Buera, Lorena | García Bartolomé, Alberto | Morán Jiménez, María Josefa | Arenas Barbero, Joaquín | Hidalgo, Beatriz | Martín, Miguel A. | Ugalde Bilbao, Cristina | Sánchez Pérez, Ricardo. Journal of proteomics, 2015 . 113:38-56. , Formato Vancouver: Marín-Buera L, García-Bartolomé A, Morán M, López-Bernardo E, Cadenas S, Hidalgo B et al. Differential proteomic profiling unveils new molecular mechanisms associated with mitochondrial complex III deficiency. J Proteomics. 2015 Jan 15;113:38-56.

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Nitric oxide compounds have different effects profiles on human articular chondrocyte metabolism.

By Arenas Barbero, Joaquín | Martín, Miguel A.. Arthritis Research & Therapy, 2013 . 15(5):R115. , Formato Vancouver: de Andrés MC, Maneiro E, Martín MA, Arenas J, Blanco FJ. Nitric oxide compounds have different effects profiles on human articular chondrocyte metabolism. Arthritis Res Ther. 2013;15(5):R115.

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